@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_head {
  this: np:hasAssertion dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_assertion;
    np:hasProvenance dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_provenance;
    np:hasPublicationInfo dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_assertion a np:Assertion .
  
  dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_provenance a np:Provenance .
  
  dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_assertion {
  miriam-gene:11093 a ncit:C16612 .
  
  lld:C1848533 a ncit:C7057 .
  
  dgn-gda:DGN92a51d8872a2b238f3aeae1a4db76dfc sio:SIO_000628 miriam-gene:11093, lld:C1848533;
    a sio:SIO_001121 .
}

dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_provenance {
  dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_assertion dcterms:description
      "[These findings suggest the possibility that the AVED syndrome may not arise from an inability of TTP to bind or to transfer alpha tocopherol, but rather from defects in other activities of the protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:15065857;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP324360.RABgV4W0htnZeA_i9aOhAc0dZU2Kamxm7cEI-mHipHQrg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:09+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}